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mp
84-88 °C (lit.)
SMILES string
Brc1cc(Br)cc(C=O)c1
InChI
1S/C7H4Br2O/c8-6-1-5(4-10)2-7(9)3-6/h1-4H
InChI key
ZLDMZIXUGCGKMB-UHFFFAOYSA-N
Related Categories
Application
Reactant involved in:
- Suzuki-Miyaura cross-coupling reactions
- Synthesis of blue fluorescent dye derivatives for organic light emitting diodes
- Sharpless kinetic resolution for the formation of Baylis-Hillman enal adducts
- Synthesis of podophyllotoxin mimetic pyridopyrazoles as anticancer agents
- Allylic alkylation
- Synthesis of C2-symmetric biphosphine ligand I
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.
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Chemistry (Weinheim an der Bergstrasse, Germany), 19(12), 3842-3845 (2013-02-21)
Double-action haloketones: A super silyl group enabled the first highly diastereoselective Mukaiyama aldol reactions of α-chloro- and α-fluoroketones with a wide range of aldehydes, providing anti-β-siloxy-α-haloketones. This process is compatible with one-pot double-aldol methodology and allows for rapid access to
Synthesis, crystal structures, and antibacterial activity of a series of hydrazone compounds derived from 4-methylbenzohydrazide.
Journal of the Chilean Chemical Society, 60(2), 2961-2965 (2015)
Bioorganic & medicinal chemistry letters, 14(22), 5569-5572 (2004-10-16)
The preparation and evaluation of novel aryl urea analogs as broad-spectrum antibacterial agents is described. Numerous compounds showed low micromolar minimum inhibitory concentrations (MIC) against both Gram-positive and Gram-negative bacteria. Selected analogs also exhibited in vivo efficacy in a lethal
Synthesis and luminescence characteristics of conjugated dendrimers with 2, 4, 6-triaryl-1, 3, 5-triazine periphery.
Journal of Polymer Science Part A: Polymer Chemistry, 44(1), 254-263 (2006)
Conformational Behavior of Conjugated Polymers With Oligo (phenylene vinylene) Side Chains.
Macromolecular Chemistry and Physics, 214(5), 538-546 (2013)
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